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P52 A novel p.glu175x premature stop mutation in the C-terminal end of HSP27 is a cause of CMT2

P52 A novel p.glu175x premature stop mutation in the C-terminal end of HSP27 is a cause of CMT2

by Rossor, A.M, Davidson, G, Houlden, H.H, Kalmar, B, Greensmith, L, Reilly, M.M
Published in Neuromuscular disorders : NMD (01.03.2012)

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Journal Article